A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269642



Internal ID20836682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83427621..83427778hg38UCSC Ensembl
chr5:82723440..82723597hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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